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preOx ColonOx

by preOx.RS GmbH Germany EUDAMED

Ref 501045Model ColonOx Darmrohr

EMDN G020102

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4260702154111RN Basic UDI-DIDate24 Nov 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
preOx - ColonOx Darmrohr
Model / Reference
ColonOx Darmrohr, 501045
Primary DI / UDI-DI
04260702154111
Basic UDI-DI
4260702154111RN
Direct Marketing DI
04260702154111
EMDN Code
G020102 Intestinal lavage tubes and sets
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005017

Other devices from preOx.RS GmbH

See all devices from preOx.RS GmbH →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
Other properties (12)
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 54e3c8cc-8ff9-4215-bf6b-f5477782af06 61 fields · synced 22 Oct 2026